Pluta Piotr, Jesionek-Kupnicka Dorota, Pluta Agnieszka, Brzozowski Kamil, Braun Marcin, Kubicka-Wołkowska Joanna, Piekarski Janusz
1 Department of Surgical Oncology, Copernicus Memorial Hospital, Lodz, Poland.
Department of Cancer Pathology, Medical University of Lodz, Lodz, Poland.
Arch Med Sci. 2019 Oct 7;19(2):343-354. doi: 10.5114/aoms.2019.88509. eCollection 2023.
Neoadjuvant treatment in locally advanced breast cancer (LABC) is intended to decrease the cancer mass, increase the likelihood of radical resection and improve survival. Resistance to chemotherapy may depend on cellular expression of anti-apoptotic proteins. XIAP and survivin are the most potent inhibitors of apoptosis (IAP), but their role in drug-induced cancer cell apoptosis remains unclear. This study was designed to evaluate the impact of pre-treatment expression of XIAP and survivin on pathological complete response and survival in LABC patients.
The study included 60 LABC patients treated with anthracycline-based chemotherapy. XIAP and survivin expression was assessed immunohistochemically in pre-treatment core biopsy specimens.
Pathological complete response was achieved in 33% of the LABC patients. Low/intermediate expression of both XIAP and survivin was significantly associated with pathological complete response ( ≤ 0.04 and < 0.001, respectively) and positively correlated with disease-free survival ( = 0.017 and < 0.001) and overall survival ( = 0.052 and < 0.001). The area under receiver operating characteristics curves (AUC) revealed predictive value of survivin expression for relapse and death in breast cancer patients (AUC = 0.63, = 0.001 and AUC = 0.8, < 0.001, respectively).
Our findings suggest that downregulation of XIAP and survivin in LABC patients might predict better treatment outcomes after anthracycline-based chemotherapy. This, in turn, may indicate XIAP and survivin proteins as potential targets for innovative anticancer therapies.
局部晚期乳腺癌(LABC)的新辅助治疗旨在减小癌块大小,增加根治性切除的可能性并提高生存率。对化疗的耐药性可能取决于抗凋亡蛋白的细胞表达。X连锁凋亡抑制蛋白(XIAP)和生存素是最有效的凋亡抑制因子(IAP),但它们在药物诱导的癌细胞凋亡中的作用仍不清楚。本研究旨在评估XIAP和生存素的预处理表达对LABC患者病理完全缓解和生存的影响。
本研究纳入了60例接受蒽环类化疗的LABC患者。通过免疫组织化学方法在预处理的粗针活检标本中评估XIAP和生存素的表达。
33%的LABC患者实现了病理完全缓解。XIAP和生存素的低/中度表达均与病理完全缓解显著相关(分别为≤0.04和<0.001),并与无病生存期(分别为=0.017和<0.001)及总生存期(分别为=0.052和<0.001)呈正相关。受试者工作特征曲线(AUC)下面积显示生存素表达对乳腺癌患者复发和死亡具有预测价值(AUC分别为0.63,=0.001和AUC为0.8,<0.001)。
我们的研究结果表明,LABC患者中XIAP和生存素的下调可能预示着蒽环类化疗后更好的治疗效果。这反过来可能表明XIAP和生存素蛋白是创新抗癌疗法的潜在靶点。